{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["K2p17.1","TALK-2","TALK2","TASK4","TASK-4"],"biotype":"protein_coding","hgnc_id":"HGNC:14465","gene_name":"potassium two pore domain channel subfamily K member 17","omim_gene":["607370"],"alias_name":null,"gene_symbol":"KCNK17","hgnc_symbol":"KCNK17","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:39266777-39282329","ensembl_id":"ENSG00000124780"}},"GRch38":{"90":{"location":"6:39299001-39314553","ensembl_id":"ENSG00000124780"}}},"hgnc_date_symbol_changed":"2001-06-29"},"entity_type":"gene","entity_name":"KCNK17","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH"],"phenotypes":[],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":506,"hash_id":null,"name":"Progressive cardiac conduction disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.28","version_created":"2019-09-09T16:10:26.535463Z","relevant_disorders":["R328"],"stats":{"number_of_genes":15,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"}]}}]}